HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157009del , CM000681.2:g.55157009del | GRCh38 |
NC_000019.9:g.55668377del , CM000681.1:g.55668377del | GRCh37 |
NC_000019.8:g.60360189del | NCBI36 |
NG_007866.2:g.5726del , LRG_432:g.5726del | |
NG_032759.1:g.14716del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.108+43del MANE Select | ENSP00000341838.5:n.108+43del | |
ENST00000665070.1:c.108+43del | ENSP00000499482.1:n.108+43del | |
ENST00000344887.9:c.108+43del | ENSP00000341838.5:n.108+43del | |
ENST00000586446.1:n.293del | ||
ENST00000586669.5:n.116+43del | ||
ENST00000587176.5:n.292+43del | ||
ENST00000587871.1:c.727+43del | ||
ENST00000590463.1:n.280+43del | ||
NM_000363.4:c.108+43del , LRG_432t1:c.108+43del | NP_000354.4:n.108+43del | |
NM_000363.5:c.108+43del MANE Select | NP_000354.4:n.108+43del |